US2017165199A1PendingUtilityA1

Dried formulations of nanoparticle-coated capsules

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Assignee: UNIV SOUTH AUSTRALIAPriority: Jun 7, 2005Filed: Sep 27, 2016Published: Jun 15, 2017
Est. expiryJun 7, 2025(expired)· nominal 20-yr term from priority
A61J 3/02A61K 8/553A23V 2002/00A61K 31/7088A61K 8/25A23P 10/35A61K 9/10A61K 47/02A61K 2800/413A61K 47/24A61K 8/63A61K 47/28A61K 38/00A61K 2800/651A61Q 17/04A61K 9/127A61K 9/1271A23L 33/115A61K 8/06A61K 8/04B01J 13/02A61K 8/11A61K 9/14B01J 13/22A61K 9/5089A61K 9/501A61K 9/1075B82Y 5/00A61K 2800/412A61K 9/5115A61Q 19/00A61J 3/005A61K 9/5192A61K 8/0241
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Claims

Abstract

A method of producing a dried formulation for an active substance such as a drug compound is described. The method involves dispersing a discontinuous phase (e.g. an oil-based or lipidic medium) comprising the active substance into a continuous phase (e.g. water) so as to form a two-phase liquid system comprising droplets of said discontinuous phase, allowing nanoparticles to congregate at the phase interface at the surface of the droplets such that at least one layer of nanoparticles coat the droplets and thereby provide sufficient structural integrity to the droplets to enable the subsequent removal of the continuous phase, and thereafter removing the continuous phase from the nanoparticle-coated droplets to produce a dried formulation.

Claims

exact text as granted — not AI-modified
1 . A dried formulation for an active substance produced by spray- or freeze-drying a dispersion of liposomes comprising a single or multiple lipid bilayer, surrounding an aqueous phase comprising said active substance, wherein said liposomes are coated with at least one layer of nanoparticles congregated at a phase interface of said liposomes. 
     
     
         2 . The formulation of  claim 1 , wherein the active substance is selected from the group consisting of nutriceutical substances, cosmetic substances and drug compounds. 
     
     
         3 . The formulation of  claim 1 , wherein the active substance is a biological agent. 
     
     
         4 . The formulation of  claim 3 , wherein the biological agent is selected from the group consisting of a peptide, a protein and a nucleic acid. 
     
     
         5 . The formulation of  claim 1 , wherein the nanoparticles have hydrophilic surfaces. 
     
     
         6 . The formulation of  claim 1 , wherein the nanoparticles are silica nanoparticles. 
     
     
         7 . The formulation of  claim 6 , wherein the nanoparticles are silica nanoparticles. 
     
     
         8 . The formulation of  claim 1 , wherein the nanoparticles have an average diameter in the range of 5-80 nm. 
     
     
         9 . The formulation of  claim 8 , wherein the nanoparticles have an average diameter of about 50 nm. 
     
     
         10 . The formulation of  claim 1 , wherein the single or multiple lipid bilayer comprises lecithin. 
     
     
         11 . The formulation of  claim 1 , wherein the single or multiple lipid bilayer comprises lecithin and cholesterol.

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